NewQuality Assurance Validation Contractor BioPharma Consulting JAD GroupQuality Assurance Validation ContractorBoston, MACollaborate with cross-functional teams (Validation, QA, Engineering, Manufacturing, QC) to support timely execution of validation projects. Team player who works well in large multi-disciplinary project groups by listening effectively and inviting open discussion.
Sr. Manager, Quality Operations (Onsite) Insulet CorpSr. Manager, Quality Operations (Onsite)Acton, MA$140,100–$210,150 / yearInsulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. As a Senior Manager, Quality Control, you''ll oversee laboratory testing, validation, lot release, compliance, and continuous improvement initiatives while leading and developing a high-performing team in a fast-paced, highly automated manufacturing environment.
NewSenior Associate, Quality Assurance Replimune Group IncSenior Associate, Quality AssuranceFramingham, MA$106,000–$137,000 / yearThe RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. Support the oversight of Replimune GMP compliance and Quality systems: change control, deviation, and corrective and preventive action (CAPA) systems including support of thorough root cause analysis investigations related to quality issues.
Senior Quality Engineer Nova Biomedical CorpSenior Quality EngineerBillerica, MA$125,000–$135,000 / yearResponsibilities: Provide expertise and general oversight for the management of Nova Biomedicals Quality Systems, including quality planning, quality control planning, internal auditing, inspection procedures, document controls, change management, process controls, quality records, corrective and preventive activities, validations, and data management. Job Summary: The Senior Quality Engineer will provide Quality Engineering support to ensure that quality practices are effectively implemented and maintained across design transfer, incoming inspection, production, field returns, and data monitoring.
SCADA Controls Automation Engineer Woodard & Curran IncSCADA Controls Automation EngineerCanton, MA$75,000–$100,000 / yearExperience with Allen-Bradley PLC hardware and software (other PLC experience is a bonus); Experience with Allen-Bradley FactoryTalk, Aveva Wonderware, Ignition and GE Proficy iFix HMI software (other HMI package experience is a bonus); Experience configuring and developing graphics for OITs such as Allen-Bradley PanelView and Automation Direct C-More; Experience with automated reporting software (such as SyTech's XLReporter and HachWims); Hands-on experience configuring, interfacing with, and troubleshooting instrumentation found in the water and wastewater industry; Experience with using electrical schematics to commission or troubleshoot a control panel; Strong electrical and mechanical aptitude; Experience with Microsoft Office suite (Teams, Word, Excel, PowerPoint); Computer networking experience (hardware and configuration) is a bonus; Experience in higher programming languages (VB, C++, Java, Python) is a bonus; Water/wastewater industry experience is a bonus. What you will need to succeed: BS in Electrical Engineering, Computer Systems Engineering, Industrial Engineering, Electrical Engineering or associated field; PE License or CAP (Certified Automation Professional) is a bonus; 2 - 3 years' experience in control system integration.
NewAssociate Director, Analytical Quality by Design and Platform Analytical Method Lifecycle 3316 Takeda Development Center AmericasAssociate Director, Analytical Quality by Design and Platform Analytical Method LifecycleLexington, MassachusettsThe Associate Director, Analytical Quality by Design and Platform Analytical Method Life Cycle plays a critical role in implementation of Analytical Quality by Design principles across Analytical Development to improve method robustness, analytical transfers, lifecycle management, and regulatory readiness. Serve as a technical and strategic lead for analytical method lifecycle practices, including risk assessments, method development expectations, validation/verification strategy, analytical transfer readiness, and continued method performance monitoring to ensure execution excellence across a diverse and dynamic global development portfolio.
Senior Manager, Quality Assurance A.W. Chesterton CompanySenior Manager, Quality AssuranceGroveland, Massachusetts$140,000–$155,000 / yearEffectively utilize quality tools to collect and interpret data to prioritize and realize improvement opportunities, i.e., Cause & Effect Diagram, Flowcharting, Check Sheets, Pareto Diagram, Histograms, Control Charts, Scatter Diagrams. These folks are our manufacturing leaders - shop managers, purchasing professionals, production and demand planners, engineers, and quality professionals who value working with other top manufacturing professionals and helping solve complex production problems.
Manager, Quality Engineering Nordson CorporationManager, Quality EngineeringSalem, NHThe Quality Engineering Manager leads a team of quality engineers, calibration specialists, inspectors, and quality team leads, ensuring effective support of manufacturing operations through risk-based decision making, statistical analysis, root cause investigations, and continuous improvement initiatives. This role serves as a key partner to operations, manufacturing engineering, supply chain, and regulatory/quality systems leadership to improve product quality, reduce Cost of Poor Quality (COPQ), drive process capability, and ensure compliance with applicable regulatory and quality system requirements.
Senior Operations Manager, Building Automation and Controls - Automated Logic Carrier CorporationSenior Operations Manager, Building Automation and Controls - Automated LogicCanton, MA$117,500–$234,500 / yearBeyond internal management, you will serve as a strategic partner to Sales, working directly with Project Managers, Field Supervisors, and external partners (such as Mechanical and Electrical contractors) to expand business opportunities, strengthen key client relationships, and ensure exceptional customer experience. Time off and Leave: Paid vacation days, up to 15 days; paid sick days, up to 5 days; paid personal leave, up to 5 days; paid holidays, up to 13 days; birth and adoption leave; parental leave; family and medical leave; bereavement leave; jury duty leave; military leave; purchased vacation.
Supplier Quality Engineer BeviSupplier Quality EngineerBoston, MA$94,690–$116,970 / yearApply an Advanced Product Quality Planning (APQP) framework to drive defect prevention at the supplier, owning the PPAP submission and approval process (PFMEA, control plan, process flow, MSA, dimensional/capability studies) for assigned parts. Serve as the lead supplier quality interface triaging field issues to root cause at the suppliers driving 8D corrective action, and verifying fixes hold against top-level quality metrics.
Quality Specialist PGI FoodsQuality SpecialistLowell, Massachusetts$20–$25 / hourFull timeIf you're passionate about quality, enjoy working as part of a team, and want to build a long-term career in food manufacturing, apply today! Partner with Quality Assurance, R&D, and Production teams to improve product consistency and manufacturing processes.
Specialist / Senior Specialist - Quality Assurance Kiniksa Pharmaceuticals CorpSpecialist / Senior Specialist - Quality AssuranceLexington, MA$107,500–$117,500 / yearWith deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent pericarditis. Experience with review of GMP manufacturing records (Master/Executed batch records, change controls, deviations, investigations, change controls, product complaints) associated with clinical programs.
Sr. Engineer, Quality - Allografts LeMaitreSr. Engineer, Quality - AllograftsBurlington, MassachusettsFull timeQualifications: Bachelors’ degree in either Biology, Microbiology, Chemistry, Chemical Engineering, Mechanical Engineering, or Biomedical Engineering required. Overview: Plans and conducts activities concerned with quality control, quality assurance and compliance of allograft processing.
Air Quality Compliance Manager Pinellas CountyAir Quality Compliance ManagerBoston, MAIf you are passionate about protecting air resources, enjoy a variety of work projects, and bring expertise in air quality compliance, enforcement and data management, this may be the perfect opportunity for you to join a stellar group of Environmental Professionals as an Environmental Program Manager 1 with Pinellas County's Division of Environmental Management (DEM). Bachelor's degree with major course work in physical, natural or biological science, environmental engineering, or related field, and five (5) years of progressively more responsible professional level experience that includes supervision or supervisor training; or an equivalent combination of education, training and/or experience.
Director, QA for QC Intellia Therapeutics IncDirector, QA for QCCambridge, MA$213,063–$260,411 / yearThis role partners closely with Analytical Development to ensure effective method design, lifecycle transfer, performance characterization, and alignment of analytical control strategies from early development through commercialization, and partners with QA GMP Operations, Global Technical Operations, Process Development, Regulatory Affairs, and external testing laboratories/CMOs. Provide Quality and technical oversight of analytical method validation, verification, lifecycle management, and method transfers in close collaboration with Analytical Development, including review of validation design, acceptance criteria, and method performance trends across novel and platform-specific assays.
Product Quality Technician Straumann Holding AGProduct Quality TechnicianMA$26.61–$32.52 / hourWe develop, manufacture, and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss. We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition.
QA Automation Engineer Creatio EMEA LTDQA Automation EngineerBoston, MATeam composition: 3 Developers, 1 QA, 1 Technical Lead, 1 Agile Coach, 1 Product OwnerResponsibilities:Create and maintain E2E automated tests with Playwright (in TypeScript)Perform exploratory and manual testing for new features and complex workflowsCover UI/API/business logic scenariosWork closely with developers and analysts to identify edge cases and improve test coverageContribute to improving our QA processes, tools, and reportingRequirements:Knowing testing techniques and applying them. Will be a plus: Experience conducting load testing of web applications; Experience with Continuous Integration tools: TeamCity, Jenkins; Test automation experience: Selenium WebDriver, Cucumber, Chai, Mocha, Selenoid/Selenium Grid; Understanding the principles of OOP.What you should expect from us:Growth & Development: Clear career paths, mentorship opportunities, and access to continuous learning to help you reach your full potential.
Sr. Aerospace Quality Engineer Analog Devices IncSr. Aerospace Quality EngineerChelmsford, MA$95,600–$131,450 / yearADI combines analog, digital, AI, and software technologies into solutions that combat climate change, reliably connect humans and the world, and help drive advancements in automation and robotics, mobility, healthcare, energy and data centers. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls.
Document Control Specialist I Cirtec Medical Corp.Document Control Specialist ILowell, MA$26–$34 / hourFull timeOur expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Provides documentation such as good manufacturing practices (GMP) and good laboratory practices (GLP) procedure manuals and change authorization in accordance with company policies and government regulations.
NewAssociate II, Plant Quality Assurance Replimune Group IncAssociate II, Plant Quality AssuranceFramingham, MA$90,000–$116,500 / yearSummary of job description: The Associate II, Plant Quality Assurance (PQA) reports to the Manager, Plant Quality Assurance and is responsible for providing day-to-day Quality oversight to support Drug Substance, Drug Product, and Quality Control operations in accordance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other applicable regulatory requirements. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.